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Hereditary Coproporphyria
Hereditary coproporphyria
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Porphyrias
(9)
Porphyria
Variegate porphyria
ALAD porphyria
Hepatoeryt- hropoietic porphyria
Erythropoietic porphyrias
Erythropoietic porphyrias
Hepatic porphyrias
Porphyria, acute intermittent
Erythropoietic protoporphyria
Porphyria cutanea tarda
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Skin conditions resulting from errors in metabolism
(86)
Congenital erythropoietic porphyria
Adrenoleuk- odystrophy
Alkaptonuria
Amyloid purpura
Amyloidosis
Amyloidosis
Apolipoprotein B deficiency
B-mannosidase deficiency
CADASIL syndrome
Calcinosis cutis
Carotenosis
Cerebrotendineous xanthomatosis
Citrullinemia
Combined hyperlipidemia
Diabetic bulla
Diabetic cheiroarthropathy
Diabetic dermadrome
Diabetic dermopathy
Dystrophic calcinosis cutis
Eruptive xanthoma
Erythropoietic porphyrias
Erythropoietic protoporphyria
Fabry disease
Familial apoprotein CII deficiency
Familial dysbetalip- oproteinemia
Familial hypertrigl- yceridemia
Farber disease
Fucosidosis
Gaucher's disease
Gout
Hartnup disease
Hepatoeryt- hropoietic porphyria
Heredofamilial amyloidosis
Hunter syndrome
Hurler syndrome
Hyaluronidase deficiency
Iatrogenic calcinosis cutis
Idiopathic scrotal calcinosis
Lafora disease
Lesch–Nyhan syndrome
Lichen amyloidosis
Limited joint mobility
Lipoprotein lipase deficiency
Macular amyloidosis
Medication-induced hyperlipop- roteinemia
Metastatic calcinosis cutis
Morquio syndrome
Myxedema
Necrobiosis lipoidica
Niemann–Pick disease
Nodular amyloidosis
Nodular xanthoma
Normolipop- roteinemic xanthomatosis
Ochronosis
Osteoma cutis
Palmar xanthoma
Phenylketonuria
Porphyria
Porphyria cutanea tarda
Porphyria, acute intermittent
Primary cutaneous amyloidosis
Primary systemic amyloidosis
Prolidase deficiency
Pseudoporphyria
Secondary cutaneous amyloidosis
Secondary systemic amyloidosis
Sialidosis
Sitosterolemia
Subepidermal calcified nodule
Tangier disease
Transient erythroporphyria of infancy
Traumatic calcinosis cutis
Tuberoeruptive xanthoma
Tumoral calcinosis
Urbach–Wiethe disease
Variegate porphyria
Verruciform xanthoma
Waxy skin
Xanthelasma
Xanthoma
Xanthoma diabeticorum
Xanthoma planum
Xanthoma striatum palmare
Xanthoma tendinosum
Xanthoma tuberosum
Xanthomatosis
Xanthomatous biliary cirrhosis
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Genetic disorders
(17)
Lucey-Driscoll syndrome
Rotor syndrome
Otospondyl- omegaepiphyseal dysplasia
X-linked sideroblastic anemia
Crigler-najjar syndrome
Crigler-najjar syndrome
Dubin-Johnson syndrome
Tyrosinemia
Hereditary disorder
Partial trisomy
Alagille syndrome
Porphyria
Variegate porphyria
ALAD porphyria
Congenital erythropoietic porphyria
Porphyria, acute intermittent
Erythropoietic protoporphyria
Porphyria cutanea tarda
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Diseases and disorders
(47)
Porphyria hereditary coproporphyria
Hemorrhagic thrombocythemia
Intraparenchymal hemorrhage
Hand-Schul- ler-Christian disease
Hansens Disease
Hansens Disease
Haverhill fever
Hereditary amyloidosis
Hemangioma
Hageman factor
Porphyria congenital erythropoietic
Hereditary hyperbilirubinemia
Protoporphyria
Chronic cold urticaria
Polyglucosan body disease adult
Hereditary-sensory and autonomic neuropathy type iii
Photosensitive epilepsy
Ehlers-danlos syndrome dermatosparaxis type
Hypertension, renovascular
Familial nephritis
Pachydermo- periostosis
Hyponatremia
Hypopituitarism
Hydronephrosis
Photodermatitis
Metabolic disorders
Hydrocephalus
Vitamin a deficiency
Hemochromatosis
Metabolic diseases
Angioedema
Pneumonic plague
FTLD
Paralysis
Alzheimer disease
Porphyria
Variegate porphyria
Congenital erythropoietic porphyria
Hepatoeryt- hropoietic porphyria
Porphyrias
Porphyria, acute intermittent
Porphyria cutanea tarda
Lucey-Driscoll syndrome
Rotor syndrome
X-linked sideroblastic anemia
Tyrosinemia
Partial trisomy
Alagille syndrome
more...
Medical terms
Neuronopathy
Idiopathic
Diseases and disorders
Hepatology
Hepatic transplant
Lucey-Driscoll syndrome
Rotor syndrome
Crigler-najjar syndrome
Dubin-Johnson syndrome
Alagille syndrome
Gastroenterology
(8)
Abdominal pain
Acute pancreatitis
Hepatic transplant
Porphyria
Dubin-Johnson syndrome
Dubin-Johnson syndrome
Hemochromatosis
Angioedema
Alagille syndrome
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Metabolism
Porphyrins
Heme metabolism intermediates
Porphobilinogen
Metabolic disorders
Metabolic diseases
Medicine
Heme arginate
Nephropathy
Pierre Robin (surgeon)
Diseases and disorders
Hepatic porphyrias
Idiopathic
EC number
Coproporphyrinogen oxidase
PROTO oxidase
Uroporphyrinogen decarboxylase
ALA dehydratase
Porphobilinogen deaminase
Hexosaminidase A
Ferrochelatase
See also
(20)
Herniation of the brain
Highly conserved sequence
Heart sounds
Heme
ALA synthase
ALA synthase
Erythropoietic
Hematin
Cutaneous porphyria
Panhematin
Light sensitivity
Autosomal dominant
Autosomal recessive
Uroporphyrinogen
Coproporphyrinogen III
The International League of Dermatological Societies
Photophobia (biology)
Abbreviated mental test score
Homogentisic acid oxidase
Cytosol
Congenital bilateral absence of vas deferens
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